We offer a series of "CTSA" instructor-led courses on all aspects of conducting human subjects research (HSR), as well as a series on budgeting for clinical trials. These courses are offered throughout the year and repeat regularly. You can register for
these courses via Skillsoft (Registration Instructions).
If you need more personalized training for your group, we’re happy to help! Please contact us to begin customizing your training.
See COMIRB’s requirements
CTSA30: External IRB Oversight - UCD Requirements and Processes
To register in advance via SkillSoft, click the button below, and sign into the "Denver | Anschutz" option with your CU credentials when prompted.
This course provides an overview of the UCD’s requirements and processes when an external IRB will provide regulatory oversight for a research study. Attendees will learn the steps of the submission process, including how InfoEd, the Human Subject Research (HSR) Portal and reviews of the External IRB Coordinators in the University’s Office of Regulatory Compliance come together, and the responsibilities of the research team. The course will also provide instruction on the processes for subsequent study changes after initial approval.